Muscle Movement, Maximized
The L360 Thigh System uses neuromuscular electrical stimulation (NMES) and functional electrical stimulation (FES) to address muscle weakness by helping to strengthen leg muscles, improve knee stability, and prevent or slow muscle loss due to disuse.
Muscle Movement, Maximized
With 3D motion detection and unique user modes, the L360 helps extend and flex the muscles in the affected leg.
See how the L360 works.
The L360 Thigh System is intended to assist extension or flexion in adult individuals with muscle weakness related to disease or injury. By electrically stimulating muscles in the affected leg to extension or flexion, the system also may improve the individual’s gait.
Reimagine Rehabilitation
The L360 Thigh System is a medical device that can help people lead more active lives after total knee replacement or anterior cruciate ligament (ACL) reconstruction surgery. Using two innovative technologies, the L360 offers important benefits such as strengthening leg muscles, preventing muscle atrophy, and relaxing muscle spasms.
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The L360 Thigh System benefits:
Strengthen leg muscles
Improve knee stability
Prevent or slow muscle atrophy
Facilitate muscle re-education
Maintain or increase joint range of motion
Increase local blood flow
Relax muscle spasms
Indications for Use: The L360 Thigh System is intended to assist knee flexion or extension in adult individuals with muscle weakness related to upper motor neuron disease/injury (e.g., stroke, damage to pathways to the spinal cord). The L360 Thigh System electrically stimulates muscles in the affected leg to provide knee flexion or extension; thus, it also may improve the individual’s gait.
The L360 Thigh System may also facilitate muscle re-education, prevent/retard disuse atrophy, maintain or increase joint range of motion, increase local blood flow, provide early post-surgical quadriceps and hamstring strengthening, improve post-surgical knee stability secondary to quadriceps and hamstring strengthening, and relax muscle spasms.
L360 Thigh System is contraindicated in patients with a demand-type cardiac pacemaker, defibrillator or any electrical implant. Do not use the system on a leg where metallic implant is directly underneath the electrodes, a cancerous lesion is present or suspected, or on a leg with regional disorder (e.g., fracture or dislocation) which could be adversely affected by motion from the stimulation. Use caution in patients with diagnosed or suspected cardiac problems or epilepsy.
Full prescribing information can be found in product labeling or at: www.bionessrehab.com/l360/safety-information.
Instructions for Use / Patient Guides and Reference Cards can be made available upon request.
Contact [email protected] or Instructions for Use / Patient Guides and Reference Cards can be made available upon request.
Contact [email protected] or 855-902-5252 to request an electronic copy. to request an electronic copy.